510(k) K212859 ยท NHI Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief
First Relief
| Applicant | Dyansys, Inc., San Mateo CA, US |
| Decision | Substantially Equivalent, Dec 20, 2021 |
| Received | Sep 8, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212859
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.